Potent NK1 antagonism by SR-140333 reduces rat colonic secretory response to immunocyte activation

被引:24
作者
Moriarty, D
Selve, N
Baird, AW
Goldhill, J
机构
[1] Natl Univ Ireland Univ Coll Dublin, Dept Vet Physiol & Biochem, Dublin 4, Ireland
[2] Natl Univ Ireland Univ Coll Dublin, Conway Inst Biomol & Biomed Res, Dublin 4, Ireland
[3] Sanofi Synthelabo, Dept Internal Med, F-92504 Rueil Malmaison, France
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2001年 / 280卷 / 04期
关键词
afferent; granulocyte; irritable bowel syndrome; inflammatory bowel disease; mast cell;
D O I
10.1152/ajpcell.2001.280.4.C852
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The potent neurokinin receptor 1 (NK1) antagonist SR-140333 has previously been shown to reduce castor oil-induced secretion in animal models. The importance of tachykinins in neuroimmune control of secretion and the effect of SR-140333 on key points in this pathway were elucidated in the present study to determine the type of intestinal dysfunction best targeted by this antagonist. Rat colonic secretion and substance P (SP) release were determined in vitro with the use of Ussing chamber and enzyme immunoassay techniques. NK1 receptors played a secretory role as receptor agonists stimulated secretion and SR-140333 antagonized the response to SP response (pK(b) = 9.2). Sensory fiber stimulation released SP and evoked a large secretion that was reduced by 69% in the presence of SR-140333 (10 nM). Likewise, mastocytes also released SP. The subsequent secretory response was reduced by 43% in the presence of SR-140333 (50 nM). SP was also released from granulocytes; however, this did not cause secretion. Functional NK3 receptors were present in the colon as senktide stimulated secretion, an effect that was increased during stress. We conclude that NK3 receptors may play a role in stress-related disorders, whereas NK1 receptors are more important in mast cell/afferent-mediated secretion.
引用
收藏
页码:C852 / C858
页数:7
相关论文
共 48 条
[1]   SELECTIVE LOCALIZATION OF VASOACTIVE-INTESTINAL-PEPTIDE AND SUBSTANCE-P IN HUMAN EOSINOPHILS [J].
ALIAKBARI, J ;
SREEDHARAN, SP ;
TURCK, CW ;
GOETZL, EJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 148 (03) :1440-1445
[2]   EXPRESSION OF TETRODOTOXIN-RESISTANT SODIUM-CHANNELS IN CAPSAICIN-SENSITIVE DORSAL-ROOT GANGLION NEURONS OF ADULT-RATS [J].
ARBUCKLE, JB ;
DOCHERTY, RJ .
NEUROSCIENCE LETTERS, 1995, 185 (01) :70-73
[3]  
BALUK P, 1995, AM J PHYSIOL, V268, P263
[4]   Characterization of functional vanilloid receptors expressed by mast cells [J].
Bíró, T ;
Maurer, M ;
Modarres, S ;
Lewin, NE ;
Brodie, C ;
Acs, G ;
Acs, P ;
Paus, R ;
Blumberg, PM .
BLOOD, 1998, 91 (04) :1332-1340
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   TACHYKININS ACTIVATE GUINEA-PIG ALVEOLAR MACROPHAGES - INVOLVEMENT OF NK2 AND NK1 RECEPTORS [J].
BRUNELLESCHI, S ;
VANNI, L ;
LEDDA, F ;
GIOTTI, A ;
MAGGI, CA ;
FANTOZZI, R .
BRITISH JOURNAL OF PHARMACOLOGY, 1990, 100 (03) :417-420
[7]   INVESTIGATION OF THE 5-HYDROXYTRYPTAMINE RECEPTOR MECHANISM MEDIATING THE SHORT-CIRCUIT CURRENT RESPONSE IN RAT COLON [J].
BUNCE, KT ;
ELSWOOD, CJ ;
BALL, MT .
BRITISH JOURNAL OF PHARMACOLOGY, 1991, 102 (04) :811-816
[8]   The capsaicin receptor: a heat-activated ion channel in the pain pathway [J].
Caterina, MJ ;
Schumacher, MA ;
Tominaga, M ;
Rosen, TA ;
Levine, JD ;
Julius, D .
NATURE, 1997, 389 (6653) :816-824
[9]   Substance P as a mediator of colonic secretory reflexes [J].
Cooke, HJ ;
Sidhu, M ;
Fox, P ;
Wang, YZ ;
Zimmermann, EM .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 272 (02) :G238-G245
[10]   PHARMACOLOGICAL CHARACTERIZATION OF NEUROKININ RECEPTORS MEDIATING ANION SECRETION IN RAT DESCENDING COLON MUCOSA [J].
COX, HM ;
TOUGH, IR ;
GRAYSON, K ;
YARROW, S .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1993, 348 (02) :172-177